A model for the photodissociation of ICN in its lowest continuum is developed and is used to predict the partitioning of available energy between translational, rotational, and vibrational energies of the recoiling fragments. The model is based on three major assumptions: (i) that only one upper electronic state is involved, (ii) that light absorption affects only the breaking C–I bond, thus allowing the upper-state potential surface to be calculated quasidiatomically from spectral and thermodynamic data, and (iii) that the mechanics of the “half-collision” of the recoiling fragments on this potential surface may be treated as classical to predict the average partitioning between translational, rotational, and vibrational energies, and by a classical-energy forced quantum oscillator approximation to predict the partitioning between vibrational states. The model predicts that most of the available energy will go into translation, which is consistent with flash photolysis studies and with crude measurements of the photofragment spectrum.
The technology for hybridization of nucleic acids using isotopically labeled whole genomic or species‐specific cloned deoxyribonucleic acid (DNA) probes for Actinobacillus actinomycetemcomitans, Bacteroides intermedius and Bacleroides gingivulis can be used to detect as few as 102 cells of these periodontal pathogens. The sensitivity and specificity of the test is not affected by the presence of 5x 10s unrelated bacteria in constructed mixed culture samples. Current feasibility tests with non‐isotopic reagents also give reliable and rapid detection of these oral pathogens in pure or mixed cultures. DNA probes should prove useful in a rapid, specific, and sensitive assay for these periodontal pathogens.
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